Dexrazoxane and Long-Term Heart Function in Survivors of Childhood Cancer

Author:

Chow Eric J.1ORCID,Aggarwal Sanjeev2,Doody David R.1ORCID,Aplenc Richard3ORCID,Armenian Saro H.4ORCID,Baker K. Scott1,Bhatia Smita5ORCID,Blythe Nancy1,Colan Steven D.6,Constine Louis S.7ORCID,Freyer David R.8ORCID,Kopp Lisa M.9,Laverdière Caroline10,Leisenring Wendy M.1ORCID,Sasaki Nao6,Vrooman Lynda M.6ORCID,Asselin Barbara L.7ORCID,Schwartz Cindy L.11ORCID,Lipshultz Steven E.12ORCID

Affiliation:

1. Fred Hutchinson Cancer Center, Seattle Children's Hospital, University of Washington, Seattle, WA

2. Children's Hospital of Michigan, Central Michigan University, Detroit, MI

3. Children's Hospital of Philadelphia, Philadelphia, PA

4. City of Hope, Duarte, CA

5. University of Alabama at Birmingham, Birmingham, AL

6. Dana-Farber Cancer Institute, Boston Children's Hospital, Boston, MA

7. University of Rochester Medical Center, Golisano Children's Hospital, Rochester, NY

8. Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA

9. University of Arizona College of Medicine, Tucson, AZ

10. Sainte-Justine University Hospital, University of Montreal, Montreal, Quebec, Canada

11. Children's Wisconsin, Medical College of Wisconsin, Milwaukee, WI

12. Department of Pediatrics, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Oishei Children's Hospital, Buffalo, NY

Abstract

PURPOSE For survivors of childhood cancer treated with doxorubicin, dexrazoxane is cardioprotective for at least 5 years. However, longer-term data are lacking. METHODS Within the Children's Oncology Group and the Dana Farber Cancer Institute's Childhood Acute Lymphoblastic Leukemia Consortium, we evaluated four randomized trials of children with acute lymphoblastic leukemia or Hodgkin lymphoma, who received doxorubicin with or without dexrazoxane, and a nonrandomized trial of patients with osteosarcoma who all received doxorubicin with dexrazoxane. Cumulative doxorubicin doses ranged from 100 to 600 mg/m2 across these five trials, and dexrazoxane was administered uniformly (10:1 mg/m2 ratio) as an intravenous bolus before doxorubicin. Cardiac function was prospectively assessed in survivors from these trials, plus a matched group of survivors of osteosarcoma treated with doxorubicin without dexrazoxane. Two-dimensional echocardiograms and blood biomarkers were analyzed centrally in blinded fashion. Multivariate analyses adjusted for demographic characteristics, cumulative doxorubicin dose, and chest radiotherapy determined the differences and associations by dexrazoxane status. RESULTS From 49 participating institutions, 195 participants were assessed at 18.1 ± 2.7 years since cancer diagnosis (51% dexrazoxane-exposed; cumulative doxorubicin dose 297 ± 91 mg/m2). Dexrazoxane administration was associated with superior left ventricular fractional shortening (absolute difference, +1.4% [95% CI, 0.3 to 2.5]) and ejection fraction (absolute difference, +1.6% [95% CI, 0.0 to 3.2]), and lower myocardial stress per B-type natriuretic peptide (–6.7 pg/mL [95% CI, –10.6 to –2.8]). Dexrazoxane was associated with a reduced risk of having lower left ventricular function (fractional shortening < 30% or ejection fraction < 50%; odds ratio, 0.24 [95% CI, 0.07 to 0.81]). This protective association was primarily seen in those treated with cumulative doxorubicin doses ≥ 250 mg/m2. CONCLUSION Among young adult-aged survivors of childhood cancer, dexrazoxane was associated with a cardioprotective effect nearly 20 years after initial anthracycline exposure.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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